Depression, Hypothalamic Pituitary Adrenal Axis, and Hippocampal and Entorhinal Cortex Volumes-The SMART Medea Study

被引:104
作者
Gerritsen, Lotte [1 ,4 ,5 ]
Comijs, Hannie C. [2 ]
van der Graaf, Yolanda [1 ]
Knoops, Arnoud J. G. [1 ,3 ]
Penninx, Brenda W. J. H. [2 ]
Geerlings, Mirjam I. [1 ]
机构
[1] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, NL-3508 GA Utrecht, Netherlands
[2] Vrije Univ Amsterdam, Med Ctr, Dept Psychiat, Extramuraal Geneeskundig Onderzoek EMGO Inst Hlth, Amsterdam, Netherlands
[3] Univ Med Ctr Utrecht, Dept Radiol, NL-3508 GA Utrecht, Netherlands
[4] Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, NL-6525 ED Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Dept Psychiat, NL-6525 ED Nijmegen, Netherlands
关键词
Cortisol; depression; entorhinal cortex; hippocampus; hypothalamic-pituitary-adrenal axis; neuroimaging; CORONARY-ARTERY-DISEASE; WHITE-MATTER LESIONS; LATE-LIFE DEPRESSION; LATE-ONSET; MAJOR DEPRESSION; BRAIN; DISORDER; STRESS; MEMORY; COGNITION;
D O I
10.1016/j.biopsych.2011.01.029
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Background: Structural brain changes have often been found in major depressive disorder (MDD), and it is thought that hypothalamic-pituitary-adrenal (HPA) axis hyperactivity may explain this relation. We investigated the association of MDD and history of depression with hippocampal and entorhinal cortex volumes and whether HPA axis activity explained this association. Methods: In 636 participants with a history of atherosclerotic disease (mean age 62 +/- 9 years, 81% male) from the second Manifestation of ARTerial disease-Memory depression and aging (SMART-Medea) study, a 12-month diagnosis of MDD and history of depression were assessed. Age of first depressive episode was classified into early-onset depression (<50 years) and late-onset depression (>= 50 years). HPA axis regulation was assessed by four morning saliva samples, two evening samples, and one awakening sample after .5 mg dexamethasone. Hippocampus and entorhinal cortex volume were manually outlined on three-dimensional T1-weighted magnetic resonance images. Results: General linear models adjusted for demographics, vascular risk, antidepressant use, and white matter lesions showed that ever having had MDD was associated with smaller hippocampal volumes but not with entorhinal cortex volumes. Remitted MDD was related to smaller entorhinal cortex volumes (p < .05). Participants with early-onset depression had smaller hippocampal volumes than those who were never depressed (p < .05), whereas participants with late-onset depression had smaller entorhinal cortex volumes (p < .05). HPA axis activity did not explain these differences. Conclusions: We found differential associations of age of onset of depression on hippocampal and entorhinal cortex volumes, which could not be explained by alterations in HPA axis regulation.
引用
收藏
页码:373 / 380
页数:8
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